Protective effects of Bidens pilosa alleviates against alcohol—induced hepatic steatosis in rats: In vivo studies and in silico analysis

Melva Silitonga , Hudson Sidabutar , Hendro Pranoto , Adriana Yulinda Dumaria LumbanGaol , Feimmy Ruth Pratiwi Sipahutar
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Abstract

Background

Steatosis has become the critical indicator of the higher alcohol exposure to liver injury. Traditional Chinese medicine, notably Bidens pilosa, is used as anti-inflammatory, antihyperglycemic, and hepatoprotective. This current study aimed to investigate the protective effect of Bidens pilosa leaves ethanolic extract (EEB) against alcohol induced hepatic steatosis.

Methods

Using the rat model of alcoholic hepatic steatosis (AHS), this study investigated EEB efficacy through the experimental analysis and in silico method. The animals received EEB at doses of 300 and 600 mg/kg for 42 days in the acute alcoholic experiment. Biochemical analysis and histopathological alteration are examined in alcohol-induced liver rats. Additionally, the pharmacological analysis, molecular docking and dynamic study were evaluated.

Results

The results indicated that the EEB has ameliorative effects against hepatic steatosis. It significantly improved hepatic histopathological change, the level of blood glucose, triglyceride, LDL and cholesterol in rats exposed to alcohol. Furthermore, the virtual screening study demonstrated the predominant compounds of EEB might regulate the top core targets linked to AHS, particularly AKT/PIK3CA, MAPK, and MTOR, respectively.

Conclusion

Thus, the preventive effect of EEB could be an underlying mechanism for the development of herbal medicine to treat AHS in clinical therapy.
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Bidens pilosa 的保护作用可减轻酒精引起的大鼠肝脂肪变性:体内研究和硅学分析
背景脂肪变性已成为较高酒精暴露对肝损伤的重要指标。传统中药,尤其是白花蛇舌草,具有抗炎、降血糖和保肝的作用。本研究旨在探讨白花蛇舌草乙醇提取物(EEB)对酒精诱导的肝脂肪变性的保护作用。方法本研究采用酒精性肝脂肪变性(AHS)大鼠模型,通过实验分析和硅学方法研究 EEB 的功效。在急性酒精中毒实验中,大鼠分别以 300 和 600 mg/kg 的剂量接受 EEB 治疗 42 天。对酒精诱导的肝脏大鼠进行生化分析和组织病理学改变研究。结果表明,EEB 对肝脏脂肪变性有改善作用。结果表明,EEB 对肝脂肪变性有改善作用,能明显改善酒精暴露大鼠的肝组织病理学变化、血糖、甘油三酯、低密度脂蛋白和胆固醇水平。此外,虚拟筛选研究表明,EEB 的主要化合物可能分别调节与 AHS 相关的顶级核心靶标,特别是 AKT/PIK3CA、MAPK 和 MTOR。
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